Canonical Allele Identifier: CA1241986458

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31091765C= , CM000664.2:g.31091765C=	GRCh38
NC_000002.11:g.31314631C= , CM000664.1:g.31314631C=	GRCh37
NC_000002.10:g.31168135C=	NCBI36
NG_051040.1:g.51962G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+46193G= MANE Select	ENSP00000288988.6:n.129+46193G=
ENST00000324589.9:c.314+22978G=	ENSP00000314500.5:n.314+22978G=
ENST00000349752.9:c.129+46193G=	ENSP00000288988.6:n.129+46193G=
ENST00000406653.5:c.69+22978G=	ENSP00000385435.1:n.69+22978G=
ENST00000424136.5:c.181+40865G=
ENST00000430167.1:c.129+46193G=	ENSP00000406399.1:n.129+46193G=
ENST00000455477.5:c.198+33389G=
ENST00000461193.5:n.164+33389G=
ENST00000464038.5:n.388+55157G=
ENST00000485468.1:n.158-12699G=
ENST00000490212.5:n.364+37512G=
ENST00000496397.5:n.202-18590G=
ENST00000498206.5:n.358+22978G=
NM_001253826.1:c.314+22978G=	NP_001240755.1:n.314+22978G=
NM_001253827.1:c.69+22978G=	NP_001240756.1:n.69+22978G=
NM_024572.3:c.129+46193G=	NP_078848.2:n.129+46193G=
NR_045602.1:n.770-12699G=
XM_011533104.1:c.315-12699G=	XP_011531406.1:n.315-12699G=
XM_011533105.1:c.69+22978G=	XP_011531407.1:n.69+22978G=
XM_011533106.1:c.42+55157G=	XP_011531408.1:n.42+55157G=
NM_001329095.1:c.-109-12699G=	NP_001316024.1:n.-109-12699G=
NM_001329096.1:c.69+22978G=	NP_001316025.1:n.69+22978G=
NM_001329097.1:c.129+46193G=	NP_001316026.1:n.129+46193G=
NM_024572.4:c.129+46193G= MANE Select	NP_078848.2:n.129+46193G=
NM_001253826.2:c.314+22978G=	NP_001240755.1:n.314+22978G=
NM_001329095.2:c.-109-12699G=	NP_001316024.1:n.-109-12699G=
NM_001329096.2:c.69+22978G=	NP_001316025.1:n.69+22978G=
NM_001329097.2:c.129+46193G=	NP_001316026.1:n.129+46193G=
NM_001253827.2:c.69+22978G=	NP_001240756.1:n.69+22978G=